1.
Indian J Pediatr
;
2006 Feb; 73(2): 161-2
Article
in English
| IMSEAR
| ID: sea-81531
ABSTRACT
Richner Hanhart syndrome is a rare inherited disorder involving the metabolism of tyrosine, a semi-essential amino acid and it should be considered in the differential diagnosis of a child presenting with ocular and skin lesions. We report a case of Richner Hanhart syndrome in a 19-month-old child, who presented with ocular and skin lesions.